Senior CRA: Site Monitoring

Clinical Research Associate II / Senior Clinical Research (CRA) - ItalyJob Category: Clinical MonitoringRequisition Number: CLINI002065Posted : October 1, 2026Full-TimeRemoteLocationsShowing 1 locationItaly - RemoteDescriptionWhatYou'llDo:Serve as main CTI contact for assigned study sitesConduct site visits (pre-study [PSV], site initiation [SIV], interim...

Overview In this role you join Medpace's Clinical Monitoring team in Italy to perform site monitoring, qualification, initiation, and closeout visits while ensuring protocol and regulatory compliance. You will verify investigator qualifications, manage data integrity, and support site performance to drive successful clinical trials. Travel up to 60-80%...

TR translational Research in Oncology (TRIO) is seeking a Senior Clinical Research Associate to join the Monitoring Resources team. The role is home-based in Italy, reporting to a CRA Line Manager, with responsibilities including site visits, regulatory compliance, data verification, and budget support.Requirements include 5+ years CRA experience, 2+ years...

Overview In this role you support multicenter clinical studies by monitoring site conduct, data integrity, and regulatory compliance to ensure study success. You collaborate with sites to recruit participants, train staff, and manage issues, while coordinating with the study team for timely execution. You will contribute to quality oversight, document...

Overview Senior Site Contracts Lead to guide site contract lifecycle across studies, ensuring compliant negotiations and templates. You will coordinate with country experts, sponsors, and the Contracts Department to manage NDAs, CTAs, amendments, and related documents. The role focuses on risk mitigation, timeline control, and regulatory alignment to enable...

Job OverviewPerform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.Essential FunctionsPerform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with...

Sponsor Dedicated CRA II/Sr CRA I/II - Home Based ITA Syneos Health®is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Every day we perform better because of how we work together,...

Fortrea seeks a Senior CRA II based in Italy to lead site monitoring and site management for clinical studies, ensuring adherence to SOPs and regulatory guidelines. The role emphasizes data integrity, regulatory compliance, and cross-functional collaboration in a multinational setting.The Sr CRA II will oversee initiation, monitoring, and close-out visits,...

Overview In this role you support multicenter clinical studies by monitoring sites to ensure protocol adherence and data reporting per GCP/ICH guidelines. You will drive site communication, training, and recruitment alignment to project needs, and manage study progress and documentation in collaboration with the study team. The role includes ensuring TMF/ISF...